Canonical Allele Identifier: PA2828462062
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1977862
ClinVar RCV Id: RCV002736836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358962.1:p.Tyr85Asp
CA382596528
NM_001372033.1:c.253T>G